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Acetic acid (R)-3-[3-(tert-butyl-dimethyl-silanyloxy)-4-nitro-butyl]-3-methyl-cyclohex-1-enylmethyl ester

Base Information
  • Chemical Name:Acetic acid (R)-3-[3-(tert-butyl-dimethyl-silanyloxy)-4-nitro-butyl]-3-methyl-cyclohex-1-enylmethyl ester
  • CAS No.:205240-90-0
  • Molecular Formula:C20H37NO5Si
  • Molecular Weight:399.603
  • Hs Code.:
Acetic acid (R)-3-[3-(tert-butyl-dimethyl-silanyloxy)-4-nitro-butyl]-3-methyl-cyclohex-1-enylmethyl ester

Synonyms:

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Chemical Property of Acetic acid (R)-3-[3-(tert-butyl-dimethyl-silanyloxy)-4-nitro-butyl]-3-methyl-cyclohex-1-enylmethyl ester
Chemical Property:
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Technology Process of Acetic acid (R)-3-[3-(tert-butyl-dimethyl-silanyloxy)-4-nitro-butyl]-3-methyl-cyclohex-1-enylmethyl ester

There total 19 articles about Acetic acid (R)-3-[3-(tert-butyl-dimethyl-silanyloxy)-4-nitro-butyl]-3-methyl-cyclohex-1-enylmethyl ester which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:
Guidance literature:
Multi-step reaction with 19 steps
1: 98 percent / sodium borohydride / ethanol / 0 °C
2: 97 percent / i-Pr2NEt, 4-DMAP / CH2Cl2 / Ambient temperature
3: 1.) O3; 2.) NaBH4 / 1.) CH2Cl2, -78 deg C; 2.) CH2Cl2, r.t.
4: Ph3P, i-PrO2CN=NCO2i-Pr / tetrahydrofuran / Ambient temperature
5: n-Bu4NF / tetrahydrofuran / Ambient temperature
6: CH2Cl2 / -78 - 20 °C / Swern oxidn.
7: NaH / 1,2-dimethoxy-ethane / Ambient temperature
8: 95 percent / H2 / Pd/C / ethanol / Ambient temperature
9: 85 percent / HCl, EtOH / 60 °C
10: 91 percent / CH2Cl2 / -78 - 20 °C / Swern oxidn.
11: 79 percent / lithium hexamethyldisilazide, HMPA / tetrahydrofuran / -78 °C
12: pyridine, 4-DMAP / Ambient temperature
13: DBU / 110 °C
14: 98 percent / diisobutylaluminum hydride / tetrahydrofuran / -78 °C
15: 97 percent / pyridine, 4-DMAP / Ambient temperature
16: (NH4)2Ce(NO3)6 / acetonitrile; H2O / 0 °C
17: -78 - 20 °C / Swern oxidn.
18: KF, 18-Crown-6 / propan-2-ol / Ambient temperature
19: 2,6-lutidine / CH2Cl2 / 0 °C
With pyridine; 2,6-dimethylpyridine; hydrogenchloride; N,N,N,N,N,N-hexamethylphosphoric triamide; dmap; potassium fluoride; sodium tetrahydroborate; ammonium cerium(IV) nitrate; 18-crown-6 ether; ethanol; di-isopropyl azodicarboxylate; tetrabutyl ammonium fluoride; hydrogen; sodium hydride; diisobutylaluminium hydride; ozone; 1,8-diazabicyclo[5.4.0]undec-7-ene; N-ethyl-N,N-diisopropylamine; triphenylphosphine; lithium hexamethyldisilazane; palladium on activated charcoal; In tetrahydrofuran; 1,2-dimethoxyethane; ethanol; dichloromethane; water; isopropyl alcohol; acetonitrile;
Guidance literature:
Multi-step reaction with 18 steps
1: 97 percent / i-Pr2NEt, 4-DMAP / CH2Cl2 / Ambient temperature
2: 1.) O3; 2.) NaBH4 / 1.) CH2Cl2, -78 deg C; 2.) CH2Cl2, r.t.
3: Ph3P, i-PrO2CN=NCO2i-Pr / tetrahydrofuran / Ambient temperature
4: n-Bu4NF / tetrahydrofuran / Ambient temperature
5: CH2Cl2 / -78 - 20 °C / Swern oxidn.
6: NaH / 1,2-dimethoxy-ethane / Ambient temperature
7: 95 percent / H2 / Pd/C / ethanol / Ambient temperature
8: 85 percent / HCl, EtOH / 60 °C
9: 91 percent / CH2Cl2 / -78 - 20 °C / Swern oxidn.
10: 79 percent / lithium hexamethyldisilazide, HMPA / tetrahydrofuran / -78 °C
11: pyridine, 4-DMAP / Ambient temperature
12: DBU / 110 °C
13: 98 percent / diisobutylaluminum hydride / tetrahydrofuran / -78 °C
14: 97 percent / pyridine, 4-DMAP / Ambient temperature
15: (NH4)2Ce(NO3)6 / acetonitrile; H2O / 0 °C
16: -78 - 20 °C / Swern oxidn.
17: KF, 18-Crown-6 / propan-2-ol / Ambient temperature
18: 2,6-lutidine / CH2Cl2 / 0 °C
With pyridine; 2,6-dimethylpyridine; hydrogenchloride; N,N,N,N,N,N-hexamethylphosphoric triamide; dmap; potassium fluoride; sodium tetrahydroborate; ammonium cerium(IV) nitrate; 18-crown-6 ether; ethanol; di-isopropyl azodicarboxylate; tetrabutyl ammonium fluoride; hydrogen; sodium hydride; diisobutylaluminium hydride; ozone; 1,8-diazabicyclo[5.4.0]undec-7-ene; N-ethyl-N,N-diisopropylamine; triphenylphosphine; lithium hexamethyldisilazane; palladium on activated charcoal; In tetrahydrofuran; 1,2-dimethoxyethane; ethanol; dichloromethane; water; isopropyl alcohol; acetonitrile;
Guidance literature:
Multi-step reaction with 17 steps
1: 1.) O3; 2.) NaBH4 / 1.) CH2Cl2, -78 deg C; 2.) CH2Cl2, r.t.
2: Ph3P, i-PrO2CN=NCO2i-Pr / tetrahydrofuran / Ambient temperature
3: n-Bu4NF / tetrahydrofuran / Ambient temperature
4: CH2Cl2 / -78 - 20 °C / Swern oxidn.
5: NaH / 1,2-dimethoxy-ethane / Ambient temperature
6: 95 percent / H2 / Pd/C / ethanol / Ambient temperature
7: 85 percent / HCl, EtOH / 60 °C
8: 91 percent / CH2Cl2 / -78 - 20 °C / Swern oxidn.
9: 79 percent / lithium hexamethyldisilazide, HMPA / tetrahydrofuran / -78 °C
10: pyridine, 4-DMAP / Ambient temperature
11: DBU / 110 °C
12: 98 percent / diisobutylaluminum hydride / tetrahydrofuran / -78 °C
13: 97 percent / pyridine, 4-DMAP / Ambient temperature
14: (NH4)2Ce(NO3)6 / acetonitrile; H2O / 0 °C
15: -78 - 20 °C / Swern oxidn.
16: KF, 18-Crown-6 / propan-2-ol / Ambient temperature
17: 2,6-lutidine / CH2Cl2 / 0 °C
With pyridine; 2,6-dimethylpyridine; hydrogenchloride; N,N,N,N,N,N-hexamethylphosphoric triamide; dmap; potassium fluoride; sodium tetrahydroborate; ammonium cerium(IV) nitrate; 18-crown-6 ether; ethanol; di-isopropyl azodicarboxylate; tetrabutyl ammonium fluoride; hydrogen; sodium hydride; diisobutylaluminium hydride; ozone; 1,8-diazabicyclo[5.4.0]undec-7-ene; triphenylphosphine; lithium hexamethyldisilazane; palladium on activated charcoal; In tetrahydrofuran; 1,2-dimethoxyethane; ethanol; dichloromethane; water; isopropyl alcohol; acetonitrile;
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